Density variation amongst mid-ocean ridge basalts: Implications for magma mixing and the scarcity of primitive lavas

Densities calculated from glass compositions of observed mid-ocean ridge basalts show that the more primitive melts are likely to be buoyant in more evolved melts. Consideration of this and other physical properties indicates that convective mixing between most basaltic magmas occurs under intermittently turbulent to turbulent conditions (transitional Reynolds Numbers) accounting for the widespread occurrence of hybrid lavas. Hypothetical picritic melts inferred to be parental to mid-ocean ridge basalts are by contrast denser than most basalts erupted on the sea floor. The most primitive basalts observed to erupt occupy a density minimum when compared to more primitive and more fractionated melts. The density minimum occurs approximately at those compositions where plagioclase and/or pyroxene join olivine as major fractionating phases. Picritic basalts are rarely erupted, because they stratify at the base of magma reservoirs.     

Amphibole-bearing basalts from the submarine volcano Kick’em-Jenny in the lesser antilles Island arc

An oceanographic survey by H.M.S. Hecla of the 1974 active submarine volcano (12°18′N and 61°38′W) revealed a crater at 190 m below sea level and bottom-sampling yielded fresh olivine basalt pyroclastics with phenocrysts of olivine, plagioclase and clinopyroxene. Megacrysts of amphilbole, up to 16 modal percent, are subsilicic and nepheline-normative ferroan pargasites. The mineral assemblage Ol+Cpx+Pl+Amph appears to have been in equilibrium in the Kick’em-Jenny melt prior to eruption, although published experimental studies on hydrous (H₂O-saturated) or anhydrous alkali basaltic compositions have not yielded this mineral assemblage at any pressure. Interpolation between the experimentally determined phase relationships for dry and water-saturated alkali basaltic liquids indicates, however, that in an isobaric section at 5 kb the observed assemblage can exist in the water-undersaturated region. The Kick’em-Jenny olivine basalts belong to a suite of variably undersaturated basaltic rocks including alkali picrites and basanites, common in Grenada and the southern Grenadines, but although the available evidence indicates the importance of the presence of water in the genesis of these melts, their origin seems most likely to be associated with partial melting of upper mantle material rather than melting of amphibolite in an underthrust lithospheric slab.     

The 1783 Lakagigar eruption in Iceland: geochemistry,CO2 and sulfur degassing

About 12.3 km³ of basaltic magma were erupted from the Lakagigar fissure in Iceland in 1783, which may have been derived from the high-level reservoir of Grimsvotn central volcano, by lateral flow within the rifted crust. We have studied the petrology of quenched, glassy tephra from sections through pyroclastic cones along the fissure. The chemical composition of matrix glass of the 1783 tephra is heterogeneous and ranges from olivine tholeiite to Fe–Ti rich basalt, but the most common magma erupted is quartz tholeiite (Mg#43.6 to 37.2). The tephra are characterized by low crystal content (5 to 9 vol%). Glass inclusions trapped in plagioclase and Fo₈₆ to Fo₇₅ olivine phenocrysts show a large range of compositions, from primitive olivine tholeiite (Mg#64.3), quartz tholeiite (Mg#43–37), to Fe–Ti basalts (Mg#33.5) which represent the most differentiated liquids and are trapped as rare melt inclusions in clinopyroxene. Both matrix glass and melt inclusion data indicate a chemically heterogeneous magma reservoir, with quartz tholeiite dominant. LREE-depleted olivine-tholeiite melt-inclusions in Mg-rich olivine and anorthitic-plagioclase phenocrysts may represent primitive magma batches ascending into the reservoir at the time of the eruption. Vesicularity of matrix glasses correlates with differentiation, ranging from 10 to 60 vol.% in evolved quartz-tholeiite glasses, whereas olivine-tholeiite glasses contain less than 10 vol.% vesicles. FTIR analyses of olivine-tholeiite melt-inclusions indicate concentrations of 0.47 wt% H₂O and 430 to 510 ppm for CO₂. Chlorine in glass inclusions and matrix glasses increases from 50 ppm in primitive tholeiite to 230 ppm in Fe–Ti basalts, without clear evidence of degassing. Melt inclusion analyses show that sulfur varies from 915 ppm to 1970 ppm, as total FeO^* increases from 9 to 13.5 wt%. Sulfur degassing correlates both with vesicularity and magma composition. Thus sulfur in matrix glasses decreases from 1490 ppm to 500 ppm, as Mg # decreases from 47 to 37 and vesicularity of the magma strongly increases. These results indicate loss of at least 75% of sulfur during the eruption. The correlation of low sulfur content in matrix glasses with high vesicularity is regarded as evidence of the control of a major exsolving volatile phase on the degassing efficiency of the magma. Our model is consistent a quasi-permanent CO₂ flux through the shallow-level magmatic reservoir of Grimsvotn. Following magma withdrawal from the reservoir and during eruption from the Lakagigar fissure, sulfur degassing was controlled by inherent CO₂-induced vesicularity of the magma.     

The 1991 eruption of Hekla,Iceland

The eruption that started in the Hekla volcano in South Iceland on 17 January 1991, and came to an end on 11 March, produced mainly andesitic lava. This lava covers 23 km² and has an estimated volume of 0.15 km³. This is the third eruption in only 20 years, whereas the average repose period since 1104 is 55 years. Earthquakes, as well as a strain pulse recorded by borehole strainmeters, occurred less than half an hour before the start of the eruption. The initial plinian phase was very short-lived, producing a total of only 0.02 km³ of tephra. The eruption cloud attained 11.5 km in height in only 10 min, but it became detached from the volcano a few hours later. Several fissures were active during the first day of the eruption, including a part of the summit fissure. By the second day, however, the activity was already essentially limited to that segment of the principal fissure where the main crater subsequently formed. The average effusion rate during the first two days of the eruption was about 800 m³ s^–1. After this peak, the effusion rate declined rapidly to 10–20 m³ s^–1, then more slowly to 1 m³ s^–1, and remained at 1–12 m³ s^–1 until the end of the eruption. Site observations near the main crater suggest that the intensity of the volcanic tremor varied directly with the force of the eruption. A notable rise in the fluorine concentration of riverwater in the vicinity of the eruptive fissures occurred on the 5th day of the eruption, but it levelled off on the 6th day and then remained essentially constant. The volume and initial silica content of the lava and tephra, the explosivity and effusion rate during the earliest stage of the eruption, as well as the magnitude attained by the associated earthquakes, support earlier suggestions that these parameters are positively related to the length of the preceeding repose period. The chemical difference between the eruptive material of Hekla itself and the lavas erupted in its vicinity can be explained in terms of a density-stratified magma reservoir located at the bottom of the crust. We propose that the shape of this reservoir, its location at the west margin of a propagating rift, and its association with a crustal weakness, all contribute to the high eruption frequency of Hekla.     

Aquifer chemistry of four high-temperature geothermal systems in Iceland

The deep water feeding wet-steam wells in four high-temperature geothermal areas in Iceland have highly variable salinity as reflected in the chlorine concentrations which vary from 20 to 19000 ppm. Using available values for equilibrium constants, the activities of 26 chemical species involving the major components of the reservoir water have been calculated and quantitative evaluations of solute/ solute, mineral/solute chemical equilibria in these geothermal systems have been made.The unflashed reservoir water is just saturated with calcite. The saline geothermal waters, which represent heated sea-water, are just saturated with anhydrite, but the dilute waters, which are of meteoric origin, are somewhat undersaturated with this mineral. The fluoride mobility is thought to be limited by an ionic exchange reaction where F^? replaces some of the OH^? in the layered silicates. The pH of the unflashed reservoir water is governed by ionic exchange equilibrium in which all the major cations participitate. At a given temperature it seems likely that the activity of one cation fixes the activities of all the other major cations and hydrogen ion. If this is so and we take all the other chemical equilibria which have been demonstrated to exist for granted, it turns out that the major element composition of the unflashed high-temperature geothermal waters is controlled by two independent variables only. These variables are the temperature and the supply to the water of the incompatible element chlorine, incompatible indicating that this element is not incorporated in the geothermal minerals.     

The chemistry of geothermal waters in Iceland. I. Calculation of aqueous speciation from 0° to 370°C

A computer programme has been developed to calculate the composition and aqueous speciation of geothermal reservoir waters including pH, redox potential and gas partial pressures. The programme is specifically suited to handle geochemical data from wet-steam wells, hot-water wells and boiling hot springs, but it may also be used for non-thermal waters. Solubility data for selected geothermal minerals are incorporated to facilitate the study of $\text{solution}\text{mineral}$ equilibria. The programme may also be used to study chemical changes in water chemistry accompanying boiling, variable degassing and cooling, and how these changes disturb $\text{solution}\text{mineral}$ equilibria.